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Study identifier: NCT07273630 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Effect of Protein Supplementation and Fluid Restriction on Plasma Sodium Levels in Patients Undergoing Pituitary Surgery

Condition: Hyponatremia · Pituitary Surgery  ·  Sponsor: University Hospital, Basel, Switzerland

PhaseNA
Planned participants282
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The investigators are conducting this study to investigate new preventive measures for patients with low sodium levels (hyponatremia), which can occur after surgery on the pituitary gland. This hyponatremia is often caused by the syndrome of inappropriate antidiuresis (SIAD). SIAD occurs when the pituitary gland secretes too much antidiuretic hormone. The antidiuretic hormone causes the kidneys to absorb more water. This dilutes the sodium in the blood and leads to hyponatremia. Low sodium levels are particularly common after pituitary surgery, as the procedure on the pituitary gland can lead to increased reactive secretion of antidiuretic hormone. At present, apart from educating patients about the symptoms of hyponatremia, there are no established standard measures for prevention after pituitary surgery. If hyponatremia is present, it is currently treated primarily by fluid restriction, which is not always pleasant or easy to adhere to. With this study, the investigators want to investigate whether protein supplementation or fluid restriction between day 4 and day 9 after surgery can serve as a preventive measure to stabilize sodium levels after pituitary surgery and improve the quality of life of patients.

This description comes directly from the study's public registry record.

Talk to the study team

Mirjam Christ-Crain, Prof. Dr. med.  ·  0041 61 328 70 80  ·  Mirjam.Christ-Crain@usb.ch

Michelle Mueller  ·  0041 61 328 55 23

Always discuss trial participation with your own doctor first.

Locations (1)

University Hospital BaselBasel, SwitzerlandRecruiting

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Source record: clinicaltrials.gov/study/NCT07273630